Bill Text: NJ A2466 | 2016-2017 | Regular Session | Amended


Bill Title: Designates month of November as "Reflex Sympathetic Dystrophy Syndrome Awareness Month" in NJ.

Spectrum: Bipartisan Bill

Status: (Engrossed - Dead) 2016-11-03 - Received in the Senate, Referred to Senate Health, Human Services and Senior Citizens Committee [A2466 Detail]

Download: New_Jersey-2016-A2466-Amended.html

[First Reprint]

ASSEMBLY, No. 2466

STATE OF NEW JERSEY

217th LEGISLATURE

 

INTRODUCED FEBRUARY 4, 2016

 


 

Sponsored by:

Assemblywoman  GAIL PHOEBUS

District 24 (Morris, Sussex and Warren)

Assemblyman  HERB CONAWAY, JR.

District 7 (Burlington)

Assemblyman  PARKER SPACE

District 24 (Morris, Sussex and Warren)

 

 

 

 

SYNOPSIS

     Designates month of November as "Reflex Sympathetic Dystrophy Syndrome Awareness Month" in NJ.

 

CURRENT VERSION OF TEXT

     As reported by the Assembly Health and Senior Services Committee on October 6, 2016, with amendments.

  


An Act designating the month of November as "Reflex Sympathetic Dystrophy Syndrome Awareness Month" in New Jersey and amending P.L.2007, c.255.

 

     Be It Enacted by the Senate and General Assembly of the State of New Jersey:

 

     1.    Section 2 of P.L.2007, c.255 (C.26:2AA-2) is amended to read as follows:

     2.    The Legislature finds and declares that:

     a.     Reflex sympathetic dystrophy syndrome (RSDS), also known as complex regional pain syndrome, is a debilitating and progressively chronic condition characterized by severe burning pain, pathological changes in bone and skin, excessive sweating, tissue swelling and extreme sensitivity to touch1[;] .1

     b.    More specifically, RSDS is thought to be a nerve disorder that generally occurs at the site of a minor or major trauma injury, but may also occur without an apparent injury to the afflicted person1[;] .1

     c.     While the causes of RSDS are unknown, the syndrome is thought to be the result of damaged nerves of the sympathetic nervous system1[;] .1

     d.    The disorder is unique in that it simultaneously affects the nerves, skin, muscles, blood vessels and bones, and if untreated, can result in permanent deformity and chronic pain1[;] .1

     e.     1[(1)]1 RSDS is often misdiagnosed because this condition is either unknown or is poorly understood; the prognosis for patients suffering from RSDS is generally much better when the condition is identified and treated as early as possible, ideally within three months of identifying the first symptoms1[; (2)] .1 Treatments aimed at relieving pain include, but are not limited to: physical therapy, medications, nerve blocks, surgical sympathectomy, spinal cord 1[stimulator] stimulation1, and transcutaneous electrical nerve 1[stimulator;] stimulation.1

     f.     If treatment is delayed, the disorder can quickly spread to the entire limb, and changes in bone and muscle may become irreversible, resulting in limited mobility, atrophy of the muscles and eventual permanent disability of patients1[; and] .1

     g.    Since a delay in diagnosis or treatment for this syndrome can result in severe physical and physiological problems, and early recognition and prompt treatment of RSDS provides the greatest opportunity for recovery, it is in the best interest of the public to establish a program to educate both individuals and medical professionals regarding this debilitative condition and to promote research to accurately identify, diagnose and treat RSDS[.] 1[; and] .1

     h.    It is appropriate to designate a month to increase public awareness and to better inform the citizens of this State about the importance of research and funding for RSDS.

     i.     It is imperative for New Jersey to commit itself to actively support public awareness and education efforts throughout the State in order to better meet the needs of its citizens who are suffering from RSDS.

(cf: P.L.2007, c.255, s.2).

 

     2.    Section 4 of P.L.2007, c.255 (C.26:2AA-4) is amended to read as follows:

     4.    a. The commissioner shall establish a reflex sympathetic dystrophy syndrome education and research program in the Department of Health.  The purpose of the program is to promote public awareness of the causes of RSDS, the value of early detection and the diagnosis of and possible treatments for the syndrome, and to promote research, through public and private sources, to accurately identify, diagnose, and treat RSDS.

     b.    The month of November each year is designated as "Reflex Sympathetic Dystrophy Syndrome Month" and the Governor is requested to annually issue a proclamation calling upon public officials and citizens of this State to observe this month with appropriate activities and programs to increase public awareness and highlight the importance of research and funding for RSDS1[; and] .1

(cf: P.L.2012, c.17, s.145)

 

     3.    This act shall take effect immediately.

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